ClinVar Miner

List of variants reported as pathogenic for thyroid cancer, nonmedullary, 1

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001079668.3(NKX2-1):c.1106C>T (p.Ala369Val)	rs537209983	0.00009
NM_000546.6(TP53):c.1118del (p.Lys373fs)	rs2150988776
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022

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